Literature DB >> 3346889

Fryns syndrome.

N Fitch.   

Abstract

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Mesh：

Year:  1988        PMID： 3346889      PMCID： PMC1015459          DOI： 10.1136/jmg.25.2.135

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

1.  Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia.

Authors:  J P Fryns
Journal:  J Med Genet       Date:  1987-05       Impact factor: 6.318

2.  Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.

Authors:  N Fitch; H Srolovitz; Y Robitaille; F Guttman
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318
  2 in total

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